Associate, Pharmacovigilance Operations/Drug Safety

Remotedxb; Dubai; On-site; AED 167,000 - 234,000; Full time

Job summary

Remotedxb in the United Arab Emirates seeks a regulatory professional to review adverse events and assist in determining regulatory reporting for assigned investigational products.

You will act as a liaison to site staff, CRAs and the case processing vendor on AE reporting issues, ensuring timely and accurate handling.

Collaborating with data management, clinical operations, regulatory affairs, quality and medical affairs, you will support end-to-end pharmacovigilance activities.

Responsibilities

• Review adverse events and assist in regulatory reporting for assigned investigational products.
• Serve as liaison to internal/external stakeholders for AE reporting issues (site staff, CRAs, vendors).
• Collaborate with data management, clinical operations, regulatory affairs, quality and medical affairs.

Job description

Responsibilities

• Responsible for reviewing adverse events and assisting in the determination of regulatory reporting for assigned investigational products
• May serve as a liaison to internal and external stakeholders for AE reporting issues (i.e. site staff, CRAs, case processing vendor)
• Works in collaboration with other functional groups such as data management, clinical operations, regulatory affairs, quality, and medical affairs